Oxidative Burst-Dependent NETosisis Is Implicated in the Resolution of Necrosis-Associated Sterile Inflammation

被引:40
作者
Biermann, Mona H. C. [1 ]
Podolska, Malgorzata J. [1 ]
Knopf, Jasmin [1 ]
Reinwald, Christiane [1 ]
Weidner, Daniela [1 ]
Maueroeder, Christian [1 ]
Hahn, Jonas [1 ]
Kienhoefer, Deborah [1 ]
Barras, Alexandre [2 ]
Boukherroub, Rabah [2 ]
Szunerits, Sabine [2 ]
Bilyy, Rostyslav [3 ]
Hoffmann, Markus [1 ]
Zhao, Yi [4 ]
Schett, Georg [1 ]
Herrmann, Martin [1 ]
Munoz, Luis E. [1 ]
机构
[1] Friedrich Alexander Univ Erlangen Nurnberg, Univ Klinikum Erlangen, Dept Internal Med Rheumatol & Immunol 3, Erlangen, Germany
[2] Univ Lille 1, IEMN, UMR CNRS 8520, Villeneuve Dascq, France
[3] Danylo Halytsky Lviv Natl Med Univ, Lvov, Ukraine
[4] Sichuan Univ, West China Hosp, Dept Rheumatol & Immunol, Chengdu, Peoples R China
基金
美国国家科学基金会;
关键词
necrosis; inflammation; nanodiamonds; NETosis; resolution; reactive oxygen species; NEUTROPHIL EXTRACELLULAR TRAPS; NADPH OXIDASE; DYING CELLS; MYELOPEROXIDASE; SIZE; NANOPARTICLES; CLEARANCE; PARTICLES; CRYSTALS; RELEASE;
D O I
10.3389/fimmu.2016.00557
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Necrosis is associated with a profound inflammatory response. The regulation of necrosis-associated inflammation, particularly the mechanisms responsible for resolution of inflammation is incompletely characterized. Nanoparticles are known to induce plasma membrane damage and necrosis followed by sterile inflammation. We observed that injection of metabolically inert nanodiamonds resulted in paw edema in WT and Ncf1** mice. However, while inflammation quickly resolved in WT mice, it persisted over several weeks in Ncf1** mice indicating failure of resolution of inflammation. Mechanistically, NOX2-dependent reactive oxygen species (ROS) production and formation of neutrophil extracellular traps were essential for the resolution of necrosis-induced inflammation: hence, by evaluating the fate of the particles at the site of inflammation, we observed that Ncf1** mice deficient in NADPH-dependent ROS failed to generate granulation tissue therefore being unable to trap the nanodiamonds. These data suggest that NOX2-dependent NETosis is crucial for preventing the chronification of the inflammatory response to tissue necrosis by forming NETosis-dependent barriers between the necrotic and healthy surrounding tissue.
引用
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页数:13
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